исо 134852003

Quality Management Systems Since 1986

Click on Industry Specific Services Below:

Key Dates for Transition to the

European Union Transition Requirement:

medical device directives must have registered to the new ISO

13485:2003 standard by July 2006.

Canadian Transition Requirements:

13488 certificate holders must have completed transition to the new

ISO 13485:2003 standard by March 14, 2006.

Manufacturing Service Organizations

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